Recall of LSL Healthcare Standard Central Line Dressing Change Kit
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
LSL Healthcare Inc. is recalling 3460 units of their Standard Central Line Dressing Change Kit due to included alcohol prep pads that were recalled for non-sterility.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on May 8, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
What Happened
LSL Healthcare Inc. is recalling medical procedure kits because they were distributed containing Webcol Large Alcohol Prep Pads, which were subsequently recalled for non-sterility.
Which Products Are Affected
The affected product is the LSL Healthcare Standard Central Line Dressing Change Kit, Model/Catalog Number: 2717J. A total of 3460 units are involved, with distribution in the states of MD, IL, and MN. The kits include Lot Code: 6A3043 with Expiration Date 11/30/2026, and Lot Code: 6B3076 with Expiration Date 01/31/2027. UDI-DI: 00661392054721; GTIN: (01)00661392054721(10)6A3043(17)261130 and (01)00661392054721(10)6B3076(17)260131. The official recall number is Z-1929-2026.
What You Should Do
Consumers should contact LSL Healthcare Inc. for instructions regarding the recall. The firm is located at 6200 W Howard St, Niles, IL 60714-3404.
Why This Matters
This recall involves medical devices that may not meet sterility standards, potentially affecting safety in healthcare procedures.
Source
Attributed to the FDA, recall number Z-1929-2026.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,091 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to May 8, 2026.
Frequently Asked Questions
Common questions about this FDA recall.